Chemical structure
Cat.No.
Product Name
CAS no.
Target
BIP-135 is a potent and selective ATP-competitiveGSK-3inhibitor, with IC50s of 16nM and 21nM for GSK-3α and GSK-3β, respectively. BIP 135 exhibits neuroprotective effect.
YN320869 Pavinetant 941690-55-7
Pavinetant (MLE-4901) is aneurokinin-3 receptor(NK3R) antagonist.
AZD-6280 is a selectiveGABAA(α2/3) receptormodulator, used for treatment of generalized anxiety disorder.
AZD7325 is a potent and orally active partial selective PAM ofGABAAα2 and Aα3 receptor(Ki=0.3 and 1.3nM, respectively), and has less antagonistic efficacy at the Aα1 and Aα5 receptor subtypes . AZD7325 is ...
A-803467 is a selective NaV1.8 channel blocker with IC50 of 8 nM, blocks tetrodotoxin-resistant currents, exhibits >100-fold selectivity against human NaV1.2, NaV1.3, NaV1.5, and NaV1.7.
FPS-ZM1 is a blood-brain-barrier permeant, non-toxic, tertiary amide compound which is a high affinity RAGE-specific inhibitor, blocking Aβ binding to the V domain of RAGE.
YN320448 GSK726701A 945721-87-9
GSK726701A is a novelprostagl and in E2 receptor 4 (EP4)partial agonist with apEC50of 7.4.
LX-1031 is a potent, orally availabletryptophan 5-hydroxylase (TPH)inhibitor that reduces serotonin (5-HT) synthesis peripherally.
RN-1734 is a selective transient receptor potential vanilloid 4 (TRPV4) antagonist with IC50 of 2.3 μM, 5.9 μM and 3.2 μM for hTRPV4, mTRPV4 and rTRPV4, respectively. RN-1734 alleviates demyelination and i...
YN320282 Piromelatine 946846-83-9
Piromelatine (Neu-P11) is amelatonin MT1/MT2receptor agonist,serotonin 5-HT1A/5-HT1Dagonist, and serotonin 5-HT2Bantagonist. Piromelatine (Neu-P11) possesses sleep promoting, analgesic, anti-neurodegenerative, anxiolytic...
YN380163 (±)-Duloxetine hydrochloride 947316-47-4
(±)-Duloxetine ((Rac)-Duloxetine) hydrochloride is the racemate of Duloxetine hydrochloride. Duloxetine hydrochloride, a serotonin-norepinephrine reuptake inhibitor, can be used for diabetic neuropathic pain and fibromyalgia as well...
WWL70 is a selectivealpha/beta hydrolase domain 6(ABHD6) inhibitor with an IC50 of 70nM.
YN482761 20(R)-Notoginsenoside R2 948046-15-9
20(R)-Notoginsenoside R2 is an isolated notoginsenoside fromPanax notoginseng.
TB5 is a potent and selective MAO-B inhibitor with Ki values of 110 and 1,450 nM for MAO-B and MAO-A, respectively.
YN373001 Duloxetine metabolite Para-N... 949095-98-1
Para-Naphthol Duloxetine is a metabolite of Duloxetine, which is a serotonin-norepinephrine reuptake inhibitor (SNRI).
YN360193 Desformylflustrabromine hydro... 951322-11-5
Desformylflustrabromine hydrochloride is a selective agonist ofα4β2neuronal nicotinic acetylcholine receptor (nAChR) with apEC50of 6.48.
YN481404 Tafamidis meglumine 951395-08-7
Tafamidis meglumine (Fx-1006A) is a potent and selectivetransthyretin (TTR)stabilizer, shows comparable potency and efficacy to the mutumant homotetramers V30M-TTR, V122I-TTR and wild t...
YN480557 Neurotoxin Inhibitor 951571-70-3
Neurotoxin Inhibitor is a neurotoxin inhibitor.
NS11394 is an orally active and unique subtype-selectiveGABAApositive allosteric receptor (PAM), with a Ki of ~0.5nM. NS11394 shows a selectivity profile in the order of GABAA-5 > α3 > α2 > α1-containing receptors. N...
MK-8998 (compound 33) is a potent and selective inhibitor of the T-typecalcium channel.
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